Slow spin relaxation of paramagnetic centers in graphene oxide

被引:29
作者
Augustyniak-Jablokow, Maria A. [1 ]
Tadyszak, Krzysztof [2 ]
Strzelczyk, Roman [1 ]
Fedaruk, Ryhor [3 ]
Carmieli, Raanan [4 ]
机构
[1] Polish Acad Sci, Inst Mol Phys, Smoluchowski Str 17, PL-60179 Poznan, Poland
[2] Adam Mickiewicz Univ, NanoBioMed Ctr, Ul Umultowska 85, PL-61614 Poznan, Poland
[3] Univ Szczecin, Inst Phys, Wielkopolska Str 15, PL-70451 Szczecin, Poland
[4] Weizmann Inst Sci, Dept Chem Res Support, IL-76100 Rehovot, Israel
关键词
TEMPERATURE QUANTUM COHERENCE; LATTICE-RELAXATION; DEAD-TIME; EPR; RESONANCE; ECHO; DEPENDENCE; REDUCTION; GRAPHITE; CRYSTALS;
D O I
10.1016/j.carbon.2019.06.024
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Paramagnetic centers in graphene oxide (GO) were studied by continuous wave and pulsed electron paramagnetic resonance (EPR) in the temperature range 4.2-300 K. Saturation of the EPR signal indicates long spin relaxation times of the paramagnetic centers and show that the relaxation times increase with lowering temperature as well as with decreasing the number of water molecules by drying. Long spin-lattice and phase memory relaxation times in deeply dried GO are quantitatively studied by the pulsed EPR techniques. The spin-lattice relaxation time is found to decrease from 52 ms at 5 K to 0.153 ms at 240 K and is dominated by the direct process below 100 K. The T-5 dependence observed at higher temperatures can result from Raman processes. The phase memory time is about 1 mu s at 240 K, changes non-monotonically with lowering temperature, and reaches its maximum of 2.2 mu s at 5 K. Molecular motions of the functional groups and the adsorbed water molecules are employed to explain this dependence. The paramagnetic centers are attributed to the unfunctionalized carbons in the highly functionalized regions of GO. Their interactions with protons are confirmed by ESEEM. Slow relaxation extends possible applications of GO for quantum computing and spintronics. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:98 / 105
页数:8
相关论文
共 65 条
[1]   Dipolar broadening and exchange narrowing of EPR lines from the paramagnetic centers distributed on a solid surface [J].
Atsarkin, VA ;
Vasneva, GA ;
Demidov, VV ;
Dzheparov, FS ;
Odintsov, BM ;
Clarkson, RB .
JETP LETTERS, 2000, 72 (07) :369-372
[2]   Room-Temperature Quantum Coherence and Rabi Oscillations in Vanadyl Phthalocyanine: Toward Multifunctional Molecular Spin Qubits [J].
Atzori, Matteo ;
Tesi, Lorenzo ;
Morra, Elena ;
Chiesa, Mario ;
Sorace, Lorenzo ;
Sessoli, Roberta .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (07) :2154-2157
[3]   Identification of a Slowly Relaxing Paramagnetic Center in Graphene Oxide [J].
Augustyniak-Jablokow, Maria A. ;
Fedaruk, Ryhor ;
Strzelczyk, Roman ;
Majchrzycki, Lukasz .
APPLIED MAGNETIC RESONANCE, 2019, 50 (06) :761-768
[4]   ESR study of spin relaxation in graphene [J].
Augustyniak-Jablokow, Maria A. ;
Tadyszak, Krzysztof ;
Mackowiak, Mariusz ;
Lijewski, Stefan .
CHEMICAL PHYSICS LETTERS, 2013, 557 :118-122
[5]   Room temperature quantum coherence in a potential molecular qubit [J].
Bader, Katharina ;
Dengler, Dominik ;
Lenz, Samuel ;
Endeward, Burkhard ;
Jiang, Shang-Da ;
Neugebauer, Petr ;
van Slageren, Joris .
NATURE COMMUNICATIONS, 2014, 5
[6]  
Balasubramanian G, 2009, NAT MATER, V8, P383, DOI [10.1038/nmat2420, 10.1038/NMAT2420]
[7]  
Barbon A, 2017, AIMS MATER SCI, V4, P147, DOI 10.3934/matersci.2017.1.147
[8]   A first principle study of graphene functionalized with hydroxyl, nitrile, or methyl groups [J].
Barhoumi, M. ;
Rocca, D. ;
Said, M. ;
Lebegue, S. .
JOURNAL OF CHEMICAL PHYSICS, 2017, 146 (04)
[9]   THEORY OF ELECTRON-SPIN RESONANCE OF MAGNETIC IONS IN METALS [J].
BARNES, SE .
ADVANCES IN PHYSICS, 1981, 30 (06) :801-938
[10]   ELECTRON SPIN-LATTICE RELAXATION MECHANISM INVOLVING TUNNELING MODES FOR TRAPPED RADICALS IN GLASSY MATRICES - THEORETICAL DEVELOPMENT AND APPLICATION TO TRAPPED ELECTRONS IN GAMMA-IRRADIATED ETHANOL GLASSES [J].
BOWMAN, MK ;
KEVAN, L .
JOURNAL OF PHYSICAL CHEMISTRY, 1977, 81 (05) :456-461